Variant report

Variant	rs4437332
Chromosome Location	chr5:68324628-68324629
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs11741340	0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11741847	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13170024	0.84[ASN][1000 genomes]
rs1981959	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4976065	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs5009394	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6450004	0.86[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6866288	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7732438	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:68320400-68327000	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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